Compound Identification
SMILES
NC1=NC2=C(N=CN2C2OC(CO)C(O)C2O)C(SSC2=NC(N)=NC3=C2N=CN3C2OC(CO)C(O)C2O)=N1
InChIKey
InChIKey=OEJGRNJVLBXXLW-UHFFFAOYSA-N
Formula
C20H24N10O8S2
Mass
596.59
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class Purine nucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Purine nucleosides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Purine nucleosides
Alternative Parents
Glycosylamines 6-thiopurines Aminopyrimidines and derivatives Monosaccharides N-substituted imidazoles Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Organic disulfides Oxacyclic compounds Azacyclic compounds Sulfenyl compounds Hydrocarbon derivatives Primary alcohols Primary amines Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-thiopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Heteroaromatic compound - Imidazole - Tetrahydrofuran - Secondary alcohol - Organic disulfide - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Primary amine - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors
Not available